Please choose an event type to view the corresponding MedsFacts report:

FATIGUE ( 54 FDA reports)
FALL ( 50 FDA reports)
DIZZINESS ( 37 FDA reports)
PAIN ( 36 FDA reports)
MULTIPLE SCLEROSIS ( 32 FDA reports)
ASTHENIA ( 31 FDA reports)
DEPRESSION ( 31 FDA reports)
INSOMNIA ( 31 FDA reports)
ANXIETY ( 29 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 29 FDA reports)
CONDITION AGGRAVATED ( 28 FDA reports)
HEADACHE ( 28 FDA reports)
DYSPHAGIA ( 27 FDA reports)
CONVULSION ( 25 FDA reports)
TREMOR ( 25 FDA reports)
CONFUSIONAL STATE ( 24 FDA reports)
GAIT DISTURBANCE ( 23 FDA reports)
DYSPNOEA ( 22 FDA reports)
HYPOAESTHESIA ( 22 FDA reports)
NAUSEA ( 22 FDA reports)
URINARY TRACT INFECTION ( 22 FDA reports)
CEREBROVASCULAR ACCIDENT ( 21 FDA reports)
ANAEMIA ( 20 FDA reports)
BONE PAIN ( 20 FDA reports)
HYPERTENSION ( 19 FDA reports)
HYPONATRAEMIA ( 19 FDA reports)
OSTEONECROSIS OF JAW ( 19 FDA reports)
VOMITING ( 19 FDA reports)
ARTHRALGIA ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
ORTHOSTATIC HYPOTENSION ( 18 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
DEHYDRATION ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
GRAND MAL CONVULSION ( 17 FDA reports)
VERTIGO ( 17 FDA reports)
ASTHMA ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
HYPOTENSION ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
OSTEOPOROSIS ( 16 FDA reports)
SPINAL OSTEOARTHRITIS ( 16 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
COGNITIVE DISORDER ( 15 FDA reports)
CONSTIPATION ( 15 FDA reports)
DYSKINESIA ( 15 FDA reports)
HICCUPS ( 15 FDA reports)
INJURY ( 15 FDA reports)
MUSCLE SPASMS ( 15 FDA reports)
BACK PAIN ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
ESCHERICHIA INFECTION ( 13 FDA reports)
MEMORY IMPAIRMENT ( 13 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
NERVOUSNESS ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
SWELLING ( 13 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 13 FDA reports)
CELLULITIS ( 12 FDA reports)
ENTEROCOCCAL INFECTION ( 12 FDA reports)
HALLUCINATION ( 12 FDA reports)
INFECTION ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
POOR DENTAL CONDITION ( 12 FDA reports)
SENSORY LOSS ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
TOOTH ABSCESS ( 12 FDA reports)
TOOTH EXTRACTION ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
BONE DISORDER ( 11 FDA reports)
BRONCHOPNEUMONIA ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
CONTUSION ( 11 FDA reports)
EXOSTOSIS ( 11 FDA reports)
GENERALISED OEDEMA ( 11 FDA reports)
GINGIVAL INFECTION ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
LUMBAR SPINAL STENOSIS ( 11 FDA reports)
LUNG DISORDER ( 11 FDA reports)
MITRAL VALVE INCOMPETENCE ( 11 FDA reports)
OSTEITIS ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PERIODONTAL DISEASE ( 11 FDA reports)
ROTATOR CUFF SYNDROME ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 11 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 11 FDA reports)
URINARY INCONTINENCE ( 11 FDA reports)
BONE OPERATION ( 10 FDA reports)
COLITIS ULCERATIVE ( 10 FDA reports)
DEATH ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
ENDODONTIC PROCEDURE ( 10 FDA reports)
MIGRAINE ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
PARANOIA ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
CATARACT ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
CHILLS ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DIVERTICULUM ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
IRRITABILITY ( 9 FDA reports)
MALAISE ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
PARKINSON'S DISEASE ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
SCLERODERMA ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
AGGRESSION ( 8 FDA reports)
AGITATION ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
APTYALISM ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
BONE DEBRIDEMENT ( 8 FDA reports)
BONE EROSION ( 8 FDA reports)
BONE FRAGMENTATION ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
COR PULMONALE CHRONIC ( 8 FDA reports)
DECUBITUS ULCER ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DEVICE FAILURE ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
DIFFICULTY IN WALKING ( 8 FDA reports)
ENTERITIS ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 8 FDA reports)
FACIAL NEURALGIA ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
GASTRODUODENITIS ( 8 FDA reports)
GINGIVAL PAIN ( 8 FDA reports)
GINGIVAL SWELLING ( 8 FDA reports)
HAEMANGIOMA ( 8 FDA reports)
HUMERUS FRACTURE ( 8 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
INJECTION SITE PAIN ( 8 FDA reports)
JOINT DISLOCATION ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
MALOCCLUSION ( 8 FDA reports)
MOUTH ULCERATION ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
OLIGURIA ( 8 FDA reports)
OSTEITIS DEFORMANS ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
OSTEOPENIA ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
PERIODONTITIS ( 8 FDA reports)
PLATELET COUNT INCREASED ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
PULPITIS DENTAL ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SCAB ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
THROMBOCYTOSIS ( 8 FDA reports)
TOOTH INJURY ( 8 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 8 FDA reports)
UTERINE ENLARGEMENT ( 8 FDA reports)
UTERINE LEIOMYOMA ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
VITREOUS DETACHMENT ( 8 FDA reports)
WEGENER'S GRANULOMATOSIS ( 8 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 7 FDA reports)
APPENDICECTOMY ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
DENTAL OPERATION ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
EYE LASER SURGERY ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
LACUNAR INFARCTION ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PATHOLOGICAL GAMBLING ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
ATELECTASIS ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BRUXISM ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
EJECTION FRACTION DECREASED ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NODULE ( 6 FDA reports)
OTITIS EXTERNA ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BRADYKINESIA ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
CRYING ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
MASS ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
OBESITY ( 5 FDA reports)
PHYSICAL DISABILITY ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
STRESS ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
COMA ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DEMENTIA WITH LEWY BODIES ( 4 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DERMATOPHYTOSIS ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HEARING DISABILITY ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPOACUSIS ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OLFACTORY NERVE DISORDER ( 4 FDA reports)
ON AND OFF PHENOMENON ( 4 FDA reports)
ORTHOSIS USER ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCAN BONE MARROW ABNORMAL ( 4 FDA reports)
SCAR ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
TEMPORAL ARTERITIS ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
TOURETTE'S DISORDER ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANGIOLIPOMA ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BREAST CANCER STAGE II ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CONGENITAL MITOCHONDRIAL CYTOPATHY ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DENTAL PROSTHESIS USER ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GROWTH RETARDATION ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
LIPOMA EXCISION ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MASS EXCISION ( 3 FDA reports)
MASTECTOMY ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 3 FDA reports)
MONONEUROPATHY MULTIPLEX ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PHLEBOLITH ( 3 FDA reports)
PITUITARY ENLARGEMENT ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
POLYP ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 3 FDA reports)
THROMBOSED VARICOSE VEIN ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE INJURY ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
VARICOSE VEIN OPERATION ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BLADDER CYST ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHLEBITIS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 2 FDA reports)
PSEUDOMONAS BRONCHITIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYOMYOSITIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CAMPTOCORMIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING PANNICULITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHIGELLA INFECTION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRAUMATIC RENAL INJURY ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

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